DRITHO-CREME HP (ANTHRALIN) CREAM [SUMMERS LABORATORIES INC]

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DRITHO-CREME HP (ANTHRALIN) CREAM [SUMMERS LABORATORIES INC]
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NDC 11086-037-01
Set ID 4d624774-3618-423c-89bd-492f4795ad19
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Summers Laboratories Inc
Generic Name
Product Class
Product Number
Application Number
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  • ACTIVE INGREDIENT

    COMPOSITION: CREAM CONTAINING ANTHRALIN U.S.P. 1.0%

  • INACTIVE INGREDIENT

    A BASE OF WHITE PETROLATUM, SODIUM LAURYL SULFATE, CETOSTEARYL ALCOHOL, ASCORBIC ACID, SALICYLIC ACID, METHYLPARABEN AND PURIFIED WATER.

  • INDICATIONS & USAGE

    INDICATION

    AN AID IN THE TOPICAL TREATMENT OF QUIESCENT OR CHRONIC PSORIASIS.

  • WARNINGS

    WARNING

    FOR EXTERNAL USE ONLY.

  • PURPOSE

    AN AID IN THE TOPICAL TREATMENT OF PSORIASIS.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN.

  • PRINCIPAL DISPLAY PANEL

    Drithocreme-1-CARTON

    DrithoCreme-1-tube

  • INGREDIENTS AND APPEARANCE
    DRITHO-CREME   HP
    anthralin cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:11086-037
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ANTHRALIN (UNII: U8CJK0JH5M) (ANTHRALIN - UNII:U8CJK0JH5M) ANTHRALIN1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11086-037-0150 g in 1 TUBE; Type 0: Not a Combination Product01/01/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2013
    Labeler - Summers Laboratories Inc (002382612)
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